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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484319생성일: 2026년 10월 26일

Carbon Dioxide → HCID 178448133, 화합물

https://huagongshe.com/reaction/484319

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2,3-DifluorophenolHCID 80879—
반응물4-Ethoxy-2,3-difluorobenzoic acidHCID 2769400—
반응물1-Ethoxy-2,3-DifluorobenzeneHCID 2782928—
반응물Diethyl sulfate potassium carbonateHCID 86747043—
반응물HCID 178448131HCID 178448131—
반응물HCID 178483778HCID 178483778—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물HCID 178448133HCID 178448133—

반응 단계

0.1 mol of 2,3-difluoro-4-ethoxybenzoic acid (preparable from 2,3-difluorophenol by alkylation using diethyl sulfate/potassium carbonate in dimethylformamide, metallation of the 2,3-difluorophenetole in the 4-position using butyllithium/tetramethylethylenediamine in tetrahydrofuran (THF) at -70° to -80° and reaction with solid carbon dioxide), 0.01 mol of 4-dimethylaminopyridine and 0.1 mol of trans-4-propylcyclohexanol are initially introduced in 150 ml of dichloromethane, a solution of 0.1 mol of dicyclohexylcarbodiimide in 30 ml of dichloromethane is added dropwise at 10° with stirring, and the mixture is subsequently stirred at room temperature for 15 hours. The mixture is filtered through silica gel with suction, the solvent is evaporated, and trans-4-propylcyclohexyl 2,3-difluoro-4-ethoxybenzoate is obtained as a residue and is purified by crystallization. Mp. 93°, cp. (48°).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05230827
출처 데이터셋uspto-grants-1993_07
ORD IDord-c0a7ba1d70d94fcfa35835ddd9b19302
출처 메모uspto-grants-1993_07